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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL1A1
(R1356H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
COL1A1
(P949S)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type I
GLikely benign
COL1A1
(A628T)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type I
+3 more
GConflicting classifications of pathogenicity
COL1A1, LOC126862586
(E288K)
Single nucleotide variant
(missense variant)
Osteogenesis imperfecta type I
+1 more
GUncertain significance
COL1A1
(P129S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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